Canonical Allele Identifier: CA1096260660
Gene: ARID1B HGNC NCBI

Linked Data

dbSNP Id: rs1778865164

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156778580_156778609dup , CM000668.2:g.156778580_156778609dup GRCh38
NC_000006.11:g.157099714_157099743dup , CM000668.1:g.157099714_157099743dup GRCh37
NC_000006.10:g.157141406_157141435dup NCBI36
NG_032093.1:g.5651_5680dup
NG_032093.2:g.5651_5680dup
NG_066624.1:g.7555_7584dup

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.900_929dup ENSP00000055163.8:p.Val310_Pro311insProGl...
ENST00000414678.8:c.900_929dup ENSP00000412835.3:p.Val310_Pro311insProGl...
ENST00000637015.2:c.900_929dup ENSP00000489729.2:p.Val310_Pro311insProGl...
ENST00000346085.10:c.900_929dup ENSP00000344546.5:p.Val310_Pro311insProGl...
ENST00000350026.10:c.651_680dup ENSP00000055163.7:p.Val227_Pro228insProGl...
ENST00000636930.2:c.900_929dup MANE Select ENSP00000490491.2:p.Val310_Pro311insProGl...
ENST00000647938.1:c.651_680dup ENSP00000498155.1:p.Val227_Pro228insProGl...
ENST00000674298.1:c.640_669dup
ENST00000346085.9:c.651_680dup ENSP00000344546.4:p.Val227_Pro228insProGl...
ENST00000350026.9:c.651_680dup ENSP00000055163.7:p.Val227_Pro228insProGl...
NM_017519.2:c.651_680dup NP_059989.2:p.Val227_Pro228insProGlyGlyGl...
NM_020732.3:c.651_680dup NP_065783.3:p.Val227_Pro228insProGlyGlyGl...
XM_005267069.3:c.651_680dup XP_005267126.2:p.Val227_Pro228insProGlyGl...
NM_001346813.1:c.651_680dup NP_001333742.1:p.Val227_Pro228insProGlyGl...
XM_011535984.2:c.651_680dup XP_011534286.2:p.Val227_Pro228insProGlyGl...
XM_017011103.2:c.651_680dup XP_016866592.1:p.Val227_Pro228insProGlyGl...
XM_017011104.1:c.651_680dup XP_016866593.1:p.Val227_Pro228insProGlyGl...
XM_017011105.2:c.651_680dup XP_016866594.1:p.Val227_Pro228insProGlyGl...
XM_017011106.2:c.651_680dup XP_016866595.1:p.Val227_Pro228insProGlyGl...
XM_017011107.2:c.651_680dup XP_016866596.1:p.Val227_Pro228insProGlyGl...
XR_002956289.1:n.734_763dup
NM_001371656.1:c.900_929dup NP_001358585.1:p.Val310_Pro311insProGlyGl...
NM_001374820.1:c.900_929dup NP_001361749.1:p.Val310_Pro311insProGlyGl...
NM_001374828.1:c.900_929dup MANE Select NP_001361757.1:p.Val310_Pro311insProGlyGl...
NM_017519.3:c.900_929dup NP_059989.3:p.Val310_Pro311insProGlyGlyGl...